Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1553883
rs1553883
1 1.000 0.040 15 82803597 intron variant A/G snv 0.83 0.700 1.000 1 2017 2017
dbSNP: rs2379994
rs2379994
1 1.000 0.040 15 82803755 intron variant T/C snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs4779064
rs4779064
1 1.000 0.040 15 82796479 intron variant C/T snv 0.15 0.700 1.000 1 2017 2017